Identification | Back Directory | [Name]
Cefdinir Glyoxalic Analog | [CAS]
79350-14-4 | [Synonyms]
Cefdinir Impurity 6 Cefdinir Impurity 12 Cefdinir Glyoxalic Analo Cefdinir Glyoxalic Analog Cefdinir Glyoxalic Analogue Cefdinir Acetaldehyde Analogue(Cefdinir Glyoxalic Analogue,Cefdinir Glyoxamide) (6R,7R)-7-(2-(2-Aminothiazol-4-yl)-2-oxoacetamido)-8-oxo-3-vinyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2-amino-4-thiazolyl)oxoacetyl]amino]-3-ethenyl-8-oxo-, (6R-trans)- (9CI) Cefdinir impurity 17/Cefdinir Acetaldehyde Analogue/Cefdinir Glyoxalic Analog/(6R,7R)-7-(2-(2-aminothiazol-4-yl)-2-oxoacetamido)-8-oxo-3-vinyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid | [Molecular Formula]
C14H12N4O5S2 | [MOL File]
79350-14-4.mol | [Molecular Weight]
380.4 |
Hazard Information | Back Directory | [Uses]
(6R,7R)-7-(2-(2-Aminothiazol-4-yl)-2-oxoacetamido)-8-oxo-3-vinyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid is used in the preparation of Cephalosporin C (C258750), an antibiotic used to study the effect of transpeptidase expression, binding, and inhibition on bacterial cell wall mucopeptide synthesis. |
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BOC Sciences
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PI & PI BIOTECH INC.
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Energy Chemical
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